Canonical Allele Identifier: CA433164565

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39435974G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394483G>A , CM000665.2:g.39394483G>A	GRCh38
NC_000003.11:g.39435974G>A , CM000665.1:g.39435974G>A	GRCh37
NC_000003.10:g.39410978G>A	NCBI36
NG_016931.1:g.16160G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000642683.1:c.651G>A	ENSP00000495376.1:p.Leu217=
ENST00000643672.1:c.648G>A	ENSP00000494532.1:p.Leu216=
ENST00000645280.1:c.645G>A	ENSP00000496690.1:p.Leu215=
ENST00000648579.1:c.755G>A	ENSP00000497638.1:p.Trp252Ter
ENST00000650617.1:c.699G>A MANE Select	ENSP00000497532.1:p.Leu233=
ENST00000273158.8:c.699G>A	ENSP00000273158.3:p.Leu233=
NM_017875.2:c.699G>A	NP_060345.2:p.Leu233=
XM_006713214.1:c.687G>A	XP_006713277.1:p.Leu229=
XM_011533869.1:c.681G>A	XP_011532171.1:p.Leu227=
XM_011533870.1:c.648G>A	XP_011532172.1:p.Leu216=
XM_011533871.1:c.519G>A	XP_011532173.1:p.Leu173=
NM_001354798.1:c.626-1915G>A	NP_001341727.1:n.626-1915G>A
NM_017875.4:c.699G>A MANE Select	NP_060345.2:p.Leu233=
XM_006713214.2:c.687G>A	XP_006713277.1:p.Leu229=
XM_011533869.2:c.681G>A	XP_011532171.1:p.Leu227=
XM_024453611.1:c.645G>A	XP_024309379.1:p.Leu215=
NM_001354798.2:c.626-1915G>A	NP_001341727.1:n.626-1915G>A